Actively Recruiting

Phase Not Applicable
Age: 60Years - 80Years
All Genders
Healthy Volunteers
NCT05048680

Effect of Hypoxic Conditioning on Cerebrovascular Health in the Elderly

Led by University Hospital, Grenoble · Updated on 2026-05-08

64

Participants Needed

1

Research Sites

254 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

In line with the ever-growing aging of Western populations, the development of preventive strategies to slow down the effects of aging on cardiovascular health represents a major challenge in order to preserve functional capacities and a sufficient quality of life in the elderly. The alteration of vascular function (at the cerebral and systemic level) with aging is an important feature in the clinical picture including a decrease in physical and cognitive capacities. Although physical activity is recognized as an essential means of combating the effects of aging, optimizing its effects by defining the most effective strategies of practice remains a key objective. Offering alternative interventions to exercise training is also necessary for people who are unwilling or unable to engage in a physical activity program. In this context, hypoxic conditioning, alone or in conjunction with rehabilitative exercise training, is a new therapeutic modality with strong preclinical validity, in particular from a cardiovascular standpoint, and used in other pathologies to improve cardiovascular function and exercise performance and quality of life. Our aim is, therefore, to investigate the effect of hypoxic conditioning (alone or in conjunction with exercise training) on cerebrovascular health in the elderly.

CONDITIONS

Official Title

Effect of Hypoxic Conditioning on Cerebrovascular Health in the Elderly

Who Can Participate

Age: 60Years - 80Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Age between 60 and 80 years
  • Physically inactive, less than 150 minutes of moderate to intense physical activity per week
  • No chronic cardiovascular, respiratory, metabolic, or neuromuscular diseases that prevent exercise or hypoxic conditioning
  • Have health coverage
  • Able to provide written informed consent
Not Eligible

You will not qualify if you...

  • Body mass index greater than 30 kg/m2
  • Smoking more than specified amount of cigarettes per day
  • Alcohol consumption exceeding 10 grams per day
  • Mental disorder or history of mental disorder
  • Taking beta-blocker medications
  • Unable or unwilling to provide informed consent
  • No health coverage
  • Exceeding annual allowance limits from other clinical trial participation
  • Deprived of freedom by judicial or administrative decision
  • Under legal protection preventing clinical trial participation

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

CHU Grenoble Alpes

La Tronche, Auvergne-Rhône-Alpes, France, 38700

Actively Recruiting

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Research Team

S

Stéphane Doutreleau, MD, PhD

CONTACT

S

Samuel Vergès, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

QUADRUPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

4

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